The ALS Association St. Louis Regional Chapter
The St. Louis Regional Chapter improves the lives of people living with ALS and their loved ones in eastern Missouri and central and southern Illinois, through services and education. We leave no stone unturned in search for the cure of this progressive neurodegenerative disease.
The ALS Association St. Louis Regional Chapter is committed to:
- Serving as a public policy advocate for people with ALS. We work on a local, state and national scale to make sure policies serve the best interests of ALS patients and caregivers, to secure funding for ALS research, and to empower patients to speak out to their representatives.
- Providing a robust, multidisciplinary approach to treatment of ALS. We have clinics throughout our service area, each with a team of doctors that can provide complete care to ALS patients — all under one roof. This multifaceted approach to care for ALS patients is scientifically proven to extend the lives of people living with ALS.
- Caring for people and families living with ALS. We provide exceptional care services and the latest resources and information for people with ALS, their families and caregivers. All of our services are provided free of charge.
